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Accogli, A. et al. (2017). A novel Xp22.13 microdeletion in Nance‐Horan syndrome. Birth defects research. 109 (11), pp. 866-868. [Online].
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Accogli, A. et al. (2017). A novel Xp22.13 microdeletion in Nance‐Horan syndrome. Birth defects research. 109 (11), pp. 866-868. [Online].